Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1060499784
rs1060499784
F8
1 1.000 0.080 X 154930646 stop gained C/T snv 0.700 0
dbSNP: rs1160914716
rs1160914716
F8
1 1.000 0.080 X 154904392 missense variant T/A snv 0.700 0
dbSNP: rs1168919288
rs1168919288
F8
1 1.000 0.080 X 154906458 missense variant C/G;T snv 0.700 0
dbSNP: rs1190563629
rs1190563629
F8
1 1.000 0.080 X 154902121 missense variant C/A snv 0.700 0
dbSNP: rs1218576358
rs1218576358
F8
1 1.000 0.080 X 154931627 missense variant C/T snv 0.700 0
dbSNP: rs1234456704
rs1234456704
F8
1 1.000 0.080 X 154966463 missense variant A/G snv 0.700 0
dbSNP: rs1240470740
rs1240470740
F8
1 1.000 0.080 X 154966004 missense variant G/A;C snv 0.700 0
dbSNP: rs1253524555
rs1253524555
F8
1 1.000 0.080 X 154953969 missense variant T/A snv 0.700 0
dbSNP: rs1258333672
rs1258333672
F8
1 1.000 0.080 X 154966101 missense variant T/A snv 0.700 0
dbSNP: rs1261929809
rs1261929809
F8
1 1.000 0.080 X 155022410 missense variant C/T snv 0.700 0
dbSNP: rs1263565590
rs1263565590
F8
1 1.000 0.080 X 154905005 missense variant C/G;T snv 0.700 0
dbSNP: rs1267586059
rs1267586059
F8
1 1.000 0.080 X 154896187 missense variant C/T snv 0.700 0
dbSNP: rs1269117966
rs1269117966
F8
1 1.000 0.080 X 154961075 missense variant C/T snv 0.700 0
dbSNP: rs1299810903
rs1299810903
F8
1 1.000 0.080 X 154953992 missense variant G/T snv 0.700 0
dbSNP: rs1304348198
rs1304348198
F8
1 1.000 0.080 X 154966016 missense variant C/T snv 0.700 0
dbSNP: rs1305924233
rs1305924233
F8
1 1.000 0.080 X 154931629 missense variant T/A;G snv 0.700 0
dbSNP: rs1320622042
rs1320622042
F8
1 1.000 0.080 X 154902101 missense variant C/T snv 0.700 0
dbSNP: rs1321311878
rs1321311878
F8
1 1.000 0.080 X 154863214 missense variant T/C snv 0.700 0
dbSNP: rs1341730743
rs1341730743
F8
1 1.000 0.080 X 154992966 missense variant G/A snv 0.700 0
dbSNP: rs1348849974
rs1348849974
F8
1 1.000 0.080 X 154899939 missense variant G/A snv 0.700 0
dbSNP: rs1364158178
rs1364158178
F8
1 1.000 0.080 X 154904390 missense variant G/C snv 0.700 0
dbSNP: rs1375894900
rs1375894900
F8
1 1.000 0.080 X 154930696 frameshift variant TTCT/- delins 0.700 0
dbSNP: rs137852354
rs137852354
F8
1 1.000 0.080 X 154837677 stop gained G/A snv 0.700 0
dbSNP: rs137852356
rs137852356
F8
1 1.000 0.080 X 154896103 stop gained G/A;T snv 5.5E-06 0.700 0
dbSNP: rs137852357
rs137852357
F8
1 1.000 0.080 X 154863161 stop gained G/A snv 0.700 0